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A Family-Based Rare Haplotype Association Method for Quantitative Traits
BACKGROUND: The variants identified in genome wide association studies account for only a small fraction of disease heritability. A key to this “missing heritability” is believed to be rare variants. Specifically, we focus on rare haplotype variant (rHTV). The existing methods for detecting rHTV are...
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| I publikationen: | Hum Hered |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6521833/ https://ncbi.nlm.nih.gov/pubmed/30799419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000493543 |
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